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Journal Abstract Search

74 related items for PubMed ID: 932535

  • 1. Chromosomal breakage and scleroderma: studies in family members.
    Emerit I, Housset E, Feingold J.
    J Lab Clin Med; 1976 Jul; 88(1):81-6. PubMed ID: 932535
    [Abstract] [Full Text] [Related]

  • 2. Chromosomal alterations in scleroderma.
    Constantin M, Leucuţia M, Purice S.
    Med Interne; 1987 Jul; 25(4):245-9. PubMed ID: 3423700
    [Abstract] [Full Text] [Related]

  • 3. Spontaneous and clastogen induced chromosomal breakage in scleroderma.
    Wolff DJ, Needleman BW, Wasserman SS, Schwartz S.
    J Rheumatol; 1991 Jun; 18(6):837-40. PubMed ID: 1716681
    [Abstract] [Full Text] [Related]

  • 4. Chromosome changes in lymphocytes of patients with scleroderma.
    Casalone R, Granata P, Minelli E, Righi R, Meroni E, Mazzola D, Sammarelli G, Baratelli E, Broggini M.
    Ann Genet; 1995 Jun; 38(3):145-50. PubMed ID: 8540685
    [Abstract] [Full Text] [Related]

  • 5. Chromosome studies in scleroderma with consideration of anticentromere antibody status and assessment of possible in vitro clastogenic activity.
    Powell FC, Schroeter AL, Winkelmann RK, Dewald GW.
    Acta Derm Venereol; 1986 Jun; 66(5):414-8. PubMed ID: 2431579
    [Abstract] [Full Text] [Related]

  • 6. [Cytogenetic findings in acute myelogenous leukemias (FAB M 1 to M 6)].
    Prösch U, Stobbe H.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1985 Jun; 112(4):481-94. PubMed ID: 2414178
    [Abstract] [Full Text] [Related]

  • 7. [Familial scleroderma with Sjogren's syndrome and lymphocyte and chromosome abnormalities].
    Camus JP, Emerit I, Reinert P, Guillien P, Crouzet J, Fourot J.
    Ann Med Interne (Paris); 1970 Feb; 121(2):149-61. PubMed ID: 5491196
    [No Abstract] [Full Text] [Related]

  • 8. [Chromosome abnormalities in systemic scleroderma].
    Emerit I, Camus JP.
    Rev Rhum Mal Osteoartic; 1972 Nov; 39(11):731-4. PubMed ID: 4654971
    [No Abstract] [Full Text] [Related]

  • 9. [Generalized scleroderma and chromosome breakage. Demonstration of a breaking factor in patients serum].
    Emerit I, Levy A, Housset E.
    Ann Genet; 1973 Jun; 16(2):135-8. PubMed ID: 4541907
    [No Abstract] [Full Text] [Related]

  • 10. Spontaneous chromosome damage (micronuclei) in systemic sclerosis and Raynaud's phenomenon.
    Porciello G, Scarpato R, Ferri C, Storino F, Cagetti F, Morozzi G, Bellisai F, Migliore L, Marcolongo R, Galeazzi M.
    J Rheumatol; 2003 Jun; 30(6):1244-7. PubMed ID: 12784397
    [Abstract] [Full Text] [Related]

  • 11. Chromosomal breakage in systemic sclerosis and related disorders.
    Emerit I.
    Dermatologica; 1976 Jun; 153(3):145-56. PubMed ID: 14037
    [Abstract] [Full Text] [Related]

  • 12. Chromosomal breakage in diffuse scleroderma. A study of 27 patients.
    Emerit I, Housset E, de Grouchy J, Camus JP.
    Rev Eur Etud Clin Biol; 1971 Jun; 16(7):684-94. PubMed ID: 5125548
    [No Abstract] [Full Text] [Related]

  • 13. Chromosome instability in human and murine autoimmune disease: anticlastogenic effect of superoxide dismutase.
    Emerit I, Michelson AM.
    Acta Physiol Scand Suppl; 1980 Jun; 492():59-65. PubMed ID: 6939306
    [Abstract] [Full Text] [Related]

  • 14. A cytogenetic analysis of twenty cases of systemic scleroderma.
    Romani F, Viguie F, Siffroi JP, Fiessenger JN.
    Ann Genet; 1986 Jun; 29(4):240-5. PubMed ID: 3495226
    [Abstract] [Full Text] [Related]

  • 15. Family studies in scleroderma (systemic sclerosis) demonstrating an HLA-linked increased chromosomal breakage rate in cultured lymphocytes.
    Rittner G, Schwanitz G, Baur MP, Black CM, Welsh KI, Kühnl P, Rittner C.
    Hum Genet; 1988 Dec; 81(1):64-70. PubMed ID: 3198128
    [Abstract] [Full Text] [Related]

  • 16. Deficient DNA repair capacity: a predisposing factor and high risk predictive marker in familial colorectal cancer.
    Ankathil R, Jyothish B, Madhavan J, Nair MK.
    J Exp Clin Cancer Res; 1999 Mar; 18(1):33-7. PubMed ID: 10374674
    [Abstract] [Full Text] [Related]

  • 17. Chromosome aberrations in Raynaud's phenomenon.
    Porciello G, Scarpato R, Storino F, Migliore L, Ferri C, Cagetti F, Morozzi G, Bellisai F, Marcolongo R, Galeazzi M.
    Eur J Dermatol; 2004 Mar; 14(5):327-31. PubMed ID: 15358572
    [Abstract] [Full Text] [Related]

  • 18. Analysis of naturally occurring and radiation-induced breakpoint locations in human chromosomes 1, 2 and 4.
    Tucker JD, Senft JR.
    Radiat Res; 1994 Oct; 140(1):31-6. PubMed ID: 7938452
    [Abstract] [Full Text] [Related]

  • 19. Prevalence of anticentromere antibody in blood relatives of anticentromere positive patients.
    Ruffatti A, Artifoni L, Glorioso S, Calligaro A, Doria A, Gambari P, Todesco S.
    J Rheumatol; 1985 Oct; 12(5):940-3. PubMed ID: 3878881
    [Abstract] [Full Text] [Related]

  • 20. Chromosomal aberrations in peripheral blood lymphocytes from patients with dermatomyositis and their first-degree relatives.
    Severin E.
    Rom J Morphol Embryol; 1995 Oct; 41(1-2):49-53. PubMed ID: 8680025
    [Abstract] [Full Text] [Related]

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